NCT07338539 BIO-SHORT: Hypofractionated RT for Poor-Prognosis GBM
| NCT ID | NCT07338539 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Tata Memorial Centre |
| Condition | Glioma |
| Study Type | INTERVENTIONAL |
| Enrollment | 108 participants |
| Start Date | 2025-11-06 |
| Primary Completion | 2031-10-27 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 108 participants in total. It began in 2025-11-06 with a primary completion date of 2031-10-27.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
High grade gliomas, particularly glioblastoma, are among the most aggressive brain tumors and are associated with poor outcomes despite standard treatment. Many patients, especially older adults or those with poor general health, are not suitable for surgery and have a life expectancy of less than 12 months. Current standard includes a shortened course of radiotherapy (over 3 weeks) combined with chemotherapy using temozolomide (TMZ), which offers limited survival benefits. This study aims to explore whether delivering radiotherapy in a shorter duration (1 or 2 weeks) at a higher dose, guided by advanced imaging with a PET scan, can improve survival in this group of patients. PET scans help identify the most active parts of the tumor, which aids in targeting of these areas more precisely, potentially improving outcomes while reducing harm to healthy brain tissue. This study will randomly assign 116 eligible patients into two groups: * One group will receive the current standard of care (3-week radiotherapy + TMZ). * The other group will receive PET-guided radiotherapy over a shorter duration (either 5 or 10 sessions) at a higher dose, alongside TMZ. The primary goal is to compare overall survival at one year between the two groups. The study will also assess how the disease progresses, side effects of treatment, and the impact on patients' quality of life. The study will be conducted over a total period of 6 years, including 4 years for patient enrolment and 2 years of follow-up. Participation in the study is entirely voluntary, and all patients will undergo an informed consent process. The study has been designed to follow all applicable ethical and regulatory guidelines. The results may help establish a more effective and convenient treatment option for patients with aggressive brain tumors and poor prognosis.
Eligibility Criteria
Inclusion Criteria: * Patients with biopsy proven IDH- wild type GBM or imaging defined GBM * Neurological Predictor Scale (NPS) = 2-3 * Unfit for surgery and referred for direct RT * Age \>/= 50 years Exclusion Criteria: * IDH mutant glioma * Histone altered glioma * Multifocal disease or Gliomatosis like appearance which necessitates whole brain RT * Disseminated disease in brain or spine * NPS = 0-1 or = 4 * Karnofsky Performance Status score less than 50(Patient requires considerable assistance and frequent medical care) * Prior administration of any systemic therapy directed against glioma (eg.Temozolomide, CCNU, Bevacizumab)
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07338539 clinical trial?
This trial is open to participants of all sexes, aged 50 Years or older, studying Glioma. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07338539 currently recruiting?
Yes, NCT07338539 is actively recruiting participants. Contact the research team at chatterji08@gmail.com for enrollment information.
Where is the NCT07338539 trial being conducted?
This trial is being conducted at Mumbai, India.
Who is sponsoring the NCT07338539 clinical trial?
NCT07338539 is sponsored by Tata Memorial Centre. The trial plans to enroll 108 participants.